ClinGen Allele Registry
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Canonical Allele Identifier:
CA15693613
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.60156035A>G
GRCh37
chr11:g.59923508A>G
Linked Data - Sequence & Population
gnomAD v2:
11:59923508 A / G
gnomAD v3:
11:60156035 A / G
gnomAD v4:
chr11-60156035-A-G
Joint Max Group AF
0.44474708 (SAS)
Genomes Max Group AF
0.44474708 (SAS)
Linked Data - NCBI & NCI
dbSNP:
983392
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.60156035A>G , CM000673.2:g.60156035A>G
GRCh38
NC_000011.9:g.59923508A>G , CM000673.1:g.59923508A>G
GRCh37
NC_000011.8:g.59680084A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'